primary ciliary dyskinesia 19 (DOID:0110608)
Alliance: disease page
Synonyms: CILD19; primary ciliary dyskinesia 19 with or without situs inversus
Alt IDs: OMIM:614935, ICD10CM:Q34.8
Definition: A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer and inner dynein arm defect, chronic sinopulmonary infections, asthenospermia, and immotile cilia and has_material_basis_in homozygous mutation in the LRRC6 gene on chromosome 8q24.